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Items: 1 to 20 of 286

1.

nsv6311310

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ADA2
Location information:
Clinical significance:
Uncertain significance,
Pathogenic
ID:
53675181
variant
2.

nsv3871425

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ADA2
Location information:
Clinical significance:
Pathogenic
ID:
48434780
variant
3.

nsv7093390

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ADA2
Location information:
Clinical significance:
Pathogenic
ID:
55267784
variant
4.

nsv4685666

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ADA2
Location information:
Clinical significance:
Likely pathogenic
ID:
50290201
variant
5.

nsv3900391

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ADA2
Location information:
Clinical significance:
Benign
ID:
48463746
variant
6.

nsv3877094

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ADA2
Location information:
Clinical significance:
Uncertain significance
ID:
48440449
variant
7.

nsv7095929

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ADA2
,
RPL32P5
Location information:
Clinical significance:
Pathogenic
ID:
55276118
variant
8.

nsv7096337

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ADA2
,
RPL32P5
Location information:
Clinical significance:
Uncertain significance
ID:
55276526
variant
9.

nsv5564411

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC107985573
,
ADA2
Location information:
Clinical significance:
Uncertain significance
ID:
52011834
variant
10.

nsv6112819

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPL32P5
,
ADA2
,
LOC107985573
Location information:
Clinical significance:
Likely pathogenic
ID:
53150664
variant
11.

nsv3880723

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC100129931
,
TADA2B
,
CCDC96
Location information:
Clinical significance:
Benign
ID:
48444078
variant
12.

nsv3874931

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
CCDC96
,
TADA2B
,
LOC100129931
Location information:
Clinical significance:
Benign
ID:
48438286
variant
13.

nsv4684305

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
DUSP14
,
SYNRG
,
LOC100419621
,
TADA2A
Location information:
Clinical significance:
Uncertain significance
ID:
50287428
variant
14.

nsv6291810

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC100419621
,
TADA2A
,
C17orf78
,
SNORA90
,
ACACA
Location information:
Clinical significance:
Uncertain significance
ID:
53637205
variant
15.

nsv4674843

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ACACA
,
C17orf78
,
LOC100419621
,
TADA2A
,
SNORA90
Location information:
Clinical significance:
Uncertain significance
ID:
50271668
variant
16.

nsv3906135

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
C17orf78
,
TADA2A
,
SNORA90
,
ACACA
Location information:
Clinical significance:
Uncertain significance
ID:
48469490
variant
17.

nsv4457405

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
ADA2
,
CECR2
,
RN7SL843P
,
CECR3
Location information:
Clinical significance:
Uncertain significance
ID:
49623040
variant
18.

nsv6311173

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
RPL32P5
,
LOC107985573
,
ADA2
Location information:
Clinical significance:
Uncertain significance
ID:
53675044
variant
19.

nsv3911811

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
PRPSAP1
,
CACNG1
,
COG1
,
LOC101928447
,
CDK3
,
MIR6783
,
LOC100507002
,
LRRC45
,
ZACN
,
LOC105371771
,
TCAM1P
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48475166
variant
20.

nsv3877950

Variant type:
copy number variation
Associated study:
nstd102
Organism:
human
Genes(s) in region:
LOC100418700
,
OR7E84P
,
MTND3P5
,
RPS24P11
,
GRPEL1
,
SMIM20
,
FAM86KP
,
LINC02261
,
DRD5
,
ATP5MGP3
,
LINC01096
,
See more...
Location information:
Clinical significance:
Pathogenic
ID:
48441305
variant
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